510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K982998Substantially Equivalent

Greiner Minicollect Serum Gel Blood Collection Tube

Greiner Meditech, Inc., Bel Air MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K982998 is the FDA 510(k) clearance record for GREINER MINICOLLECT SERUM GEL BLOOD COLLECTION TUBE, a class II device, cleared for Greiner Meditech, Inc. on under FDA product code JKA (Tubes, Vials, Systems, Serum Separators, Blood Collection). FDA records list 10 510(k) clearances for Greiner Meditech, Inc., from to . As of , FDA records show no recalls naming K982998.

Clearance record

Decision date
Received
(55 days to decision)
Product code
JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
Regulation
21 CFR 862.1675
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Greiner Meditech, Inc. 260 Gateway Dr., Suite 17a, Bel Air MD
510(k) summary
Summary
Third party review
No

Clearances, product code JKA

Trailing 12 months
6 clearances under product code JKA in the twelve months to October 2026, April 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code JKA, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20263
May 20260
June 20261
July 20260
August 20260
September 20261
October 20260